Instituto de Parasitología y Biomedicina López-Neyra, CSIC, Granada, Spain.
Hum Immunol. 2010 May;71(5):515-9. doi: 10.1016/j.humimm.2010.02.005. Epub 2010 Mar 7.
Recently, the signal transducer and activator of transcription 4 (STAT4) gene has been associated with multiple autoimmune diseases. Interestingly, a recent work showed that the T allele of the rs7574865 STAT4 SNP was associated with inflammatory bowel disease (IBD) in a Spanish population. The aim of the present study was to reevaluate the role of the STAT4 rs7574865 polymorphism on IBD. The present case-control study included 498 Crohn's disease (CD) patients, 402 ulcerative colitis (UC) patients, and 1296 healthy matched controls. Genotyping was performed using a PCR system with a pre-developed TaqMan allelic discrimination assay for the rs7574865 STAT4 SNP. Moreover, a meta-analysis was performed with the previous work in a Spanish population and the current study, including a final sample size of 1574 IBD patients (820 with CD and 754 with UC) and 2012 healthy controls. No evidence of association was found for the current case-control study (CD: p = 0.23, OR = 0.9, 95% CI = 0.75-1.1; UC: p = 0.17, OR = 1.14, 95% CI = 0.95-1.38). However, the meta-analysis showed that the STAT4 rs7574865 T allele was significantly associated with susceptibility to UC (p = 0.012 pooled; OR = 1.20, 95% CI = 1.04-1.39) but not CD (p = 0.71 pooled; OR = 0.93, 95% CI = 0.65-1.34). Our data suggest that the rs7574865 STAT4 SNP is a genetic susceptibility variant for UC but not CD in the Spanish population.
最近,信号转导子和转录激活子 4(STAT4)基因与多种自身免疫性疾病有关。有趣的是,最近的一项研究表明,西班牙人群中 STAT4 SNP 的 rs7574865T 等位基因与炎症性肠病(IBD)有关。本研究旨在重新评估 STAT4 rs7574865 多态性对 IBD 的作用。本病例对照研究纳入了 498 例克罗恩病(CD)患者、402 例溃疡性结肠炎(UC)患者和 1296 名健康匹配对照。采用 PCR 系统进行基因分型,该系统使用预开发的 TaqMan 等位基因鉴别检测用于 rs7574865STAT4 SNP。此外,对来自西班牙人群的先前研究和当前研究进行了荟萃分析,包括最终样本量为 1574 例 IBD 患者(820 例 CD 和 754 例 UC)和 2012 名健康对照。当前病例对照研究未发现关联(CD:p=0.23,OR=0.9,95%CI=0.75-1.1;UC:p=0.17,OR=1.14,95%CI=0.95-1.38)。然而,荟萃分析表明,STAT4 rs7574865T 等位基因与 UC 的易感性显著相关(p=0.012 合并;OR=1.20,95%CI=1.04-1.39),但与 CD 无关(p=0.71 合并;OR=0.93,95%CI=0.65-1.34)。我们的数据表明,在西班牙人群中,rs7574865STAT4 SNP 是 UC 的遗传易感变异,但不是 CD 的遗传易感变异。